Philips Consumer Lifestyle B.V. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Philips Consumer Lifestyle B.V. has 2 FDA 510(k) cleared medical devices. Based in Drachten, NL.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Philips Consumer Lifestyle B.V. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Philips Personal Health, A Subsidiary of Philips and Philips Personal Health, Philips North America, LLC.
2 devices